301644-20-2 Usage
Benz[g]indazole Core
Contains a benz[g]indazole core structure.
Functional Groups
Acetamide at the 2 position: Indicates the presence of a carbonyl group (C=O) attached to an amine group (NH2) at the 2 position of the benz[g]indazole core.
Phenylamino at the 3 position: Refers to an amino group (NH2) attached to a phenyl ring at the 3 position of the benz[g]indazole core.
Phenylmethyl at the 3 position: Signifies a methyl group (CH3) attached to a phenyl ring at the 3 position of the benz[g]indazole core.
DihydroStructure
Implies that the molecule contains two fewer hydrogen atoms compared to the parent compound, suggesting saturation or reduction of double bonds.
Potential Applications
Pharmaceutical or industrial applications may exist, though specific properties and potential uses require further investigation.
Check Digit Verification of cas no
The CAS Registry Mumber 301644-20-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,0,1,6,4 and 4 respectively; the second part has 2 digits, 2 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 301644-20:
(8*3)+(7*0)+(6*1)+(5*6)+(4*4)+(3*4)+(2*2)+(1*0)=92
92 % 10 = 2
So 301644-20-2 is a valid CAS Registry Number.
301644-20-2Relevant articles and documents
N-Substituted 3-(arylamino)-4,5-dihydro-2H-benz[g]indazol-2-yl acetamides with anti-inflammatory and analgesic activities
Schenone, Silvia,Bruno, Olga,Ranise, Angelo,Bondavalli, Francesco,Falcone, Giuseppe,Filippelli, Walter,Rivaldi, Barbara
, p. 383 - 388 (2007/10/03)
A series of substituted 3-(arylamino)-4,5-dihydro-2H-benz[g]indazol-2-yl acetamides was synthesized and tested in comparison with former analogues. The title compounds showed only weak antiarrhythmic properties but good anti- inflammatory and antinociceptive activity, particularly evident in the morpholino derivative. (C) 2000 Published by Elsevier Science S.A.
A poison 
